School of Chemical Engineering and Technology, Key Laboratory of Systems Bioengineering of Ministry of Education, Tianjin University, Tianjin 300072, China.
Carbohydr Polym. 2013 Nov 6;98(2):1326-34. doi: 10.1016/j.carbpol.2013.08.005. Epub 2013 Aug 7.
Intracellular delivery of native, active proteins is challenging due to the fragility of most proteins. Herein, a novel polymer/protein polyion complex (PIC) nanoparticle with core-shell structure was prepared. Carboxymethyl chitosan-grafted-terminal carboxyl group-poly(amidoamine) (CM-chitosan-PAMAM) dendrimers were synthesized by amidation and saponification reactions. (1)H NMR was used to characterize CM-chitosan-PAMAM dendrimers. The TEM images and results of lysozyme loading efficiency indicated that CM-chitosan-PAMAM dendrimers could self-assemble into core-shell nanoparticles, and lysozyme was efficiently encapsulated inside the core of CM-chitosan-PAMAM dendrimer nanoparticles. Activity of lysozyme was completely inhibited by CM-chitosan-PAMAM Dendrimers at physiological pH, whereas it was released into the medium and exhibited a significant enzymatic activity in an acidic intracellular environment. Moreover, the CM-chitosan-PAMAM dendrimer nanoparticles did not exhibit significant cytotoxicity in the range of concentrations below 3.16 mg/ml. The results indicated that these CM-chitosan-PAMAM dendrimers have excellent properties as highly potent and non-toxic intracellular protein carriers, which would create opportunities for novel applications in protein delivery.
由于大多数蛋白质的脆弱性,天然、活性蛋白质的细胞内传递具有挑战性。在此,制备了一种具有核壳结构的新型聚合物/蛋白质聚离子复合物(PIC)纳米粒子。通过酰胺化和皂化反应合成了接枝末端羧基的羧甲基壳聚糖-聚(酰胺-胺)(CM-chitosan-PAMAM)树枝状大分子。(1)H NMR 用于表征 CM-chitosan-PAMAM 树枝状大分子。溶菌酶负载效率的 TEM 图像和结果表明,CM-chitosan-PAMAM 树枝状大分子可以自组装成核壳纳米粒子,并且溶菌酶被有效地包封在 CM-chitosan-PAMAM 树枝状大分子纳米粒子的核内。在生理 pH 下,CM-chitosan-PAMAM 树枝状大分子完全抑制了溶菌酶的活性,而在酸性细胞内环境中,它被释放到介质中并表现出显著的酶活性。此外,在低于 3.16mg/ml 的浓度范围内,CM-chitosan-PAMAM 树枝状大分子纳米粒子没有表现出显著的细胞毒性。结果表明,这些 CM-chitosan-PAMAM 树枝状大分子作为高效、无毒的细胞内蛋白质载体具有优异的性能,这将为蛋白质递药的新应用创造机会。